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开发离散选择实验问卷,以调查孕妇和政策制定者对扩展无创产前筛查的偏好。

Development of a discrete choice experiment questionnaire to elicit preferences by pregnant women and policymakers for the expansion of non-invasive prenatal screening.

机构信息

Département de Médecine Sociale et Préventive, Université Laval, Québec, Canada.

Centre de Recherche du CHU de Québec, Université Laval, Québec, Canada.

出版信息

PLoS One. 2023 Jun 23;18(6):e0287653. doi: 10.1371/journal.pone.0287653. eCollection 2023.

Abstract

OBJECTIVE

An instrument for measuring intervention preferences applicable to both patients and policymakers would make it possible to better confront the needs of the supply and demand sides of the health care system. This study aimed to develop a discrete choice experiments (DCE) questionnaire to elicit the preferences of patients and policymakers. The instrument was specifically developed to estimate preferences for new conditions to be added to a screening program for fetal chromosomal anomalies.

METHODS

A DCE development study was conducted. The methods employed included a literature review, a qualitative study (based on individual semi-structured interviews, consultations, and a focus group discussion) with pregnant women and policymakers, and a pilot project with 33 pregnant women to validate the first version of the instrument and test the feasibility of its administration.

RESULTS

An initial list of 10 attributes was built based on a literature review and the qualitative research components of the study. Five attributes were built based on the responses provided by the participants from both groups. Eight attributes were consensually retained. A pilot project performed on 33 pregnant women led to a final instrument containing seven attributes: 'conditions to be screened', 'test performance', 'moment at gestational age to obtain the test result', 'degree of test result certainty to the severity of the disability', 'test sufficiency', 'information provided from test result', and 'cost related to the test'.

CONCLUSION

It is possible to reach a consensus on the construction of a DCE instrument intended to be administered to pregnant women and policymakers. However, complete validation of the consensual instrument is limited because there are too few voting members of health technology assessment agencies committees to statistically ascertain the relevance of the attributes and their levels.

摘要

目的

一种适用于患者和决策者的干预偏好测量工具,将使我们能够更好地应对医疗保健系统供需双方的需求。本研究旨在开发一种离散选择实验(DCE)问卷,以了解患者和决策者的偏好。该工具是专门为评估新条件添加到胎儿染色体异常筛查计划中而开发的。

方法

进行了一项 DCE 开发研究。所采用的方法包括文献回顾、对孕妇和决策者进行的定性研究(基于个人半结构化访谈、咨询和焦点小组讨论),以及对 33 名孕妇进行的试点项目,以验证工具的第一版并测试其管理的可行性。

结果

根据文献回顾和研究的定性研究部分,建立了一个包含 10 个属性的初始清单。根据来自两组参与者的回复,构建了 5 个属性。一致保留了 8 个属性。对 33 名孕妇进行的试点项目导致最终工具包含七个属性:“要筛查的条件”、“测试性能”、“获得测试结果的妊娠龄时刻”、“测试结果确定性与残疾严重程度的关系”、“测试充分性”、“测试结果提供的信息”和“与测试相关的成本”。

结论

可以就旨在向孕妇和决策者施测的 DCE 工具的构建达成共识。然而,由于健康技术评估机构委员会的投票成员太少,无法从统计学上确定属性及其水平的相关性,因此共识工具的完整验证受到限制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dc1a/10289448/6ec4f400cb46/pone.0287653.g001.jpg

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